The genetic basis of the Pierre Robin Sequence

Cleft Palate-Craniofacial Journal

Volumn 43, Issue 2, 2006, Pages 155-159

  Jakobsen, Linda P ^a,b   Knudsen, Mary A ^a   Lespinasse, James ^c   Ayuso, Carmen García ^d   Ramos, Carmen ^d   Fryns, Jean Pierre ^e   Bugge, Merete ^b   Tommerup, Niels ^b  

^a Mental Health Services CPH   (Denmark)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

^c GENERAL HOSPITAL   (France)

^d Hospital UniversitarioFundación Jiménez Díaz   (Spain)

^e UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Chromosomes; Craniofacial anomalies; Etiology; Genetics; Pierre Robin Sequence

Indexed keywords

TRANSCRIPTION FACTOR SOX9;

ARTICLE; CHROMOSOME 11Q; CHROMOSOME 17Q; CHROMOSOME 2Q; CHROMOSOME 4Q; CLEFT PALATE; CYTOGENETICS; GENE; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; MICROGNATHIA; ONLINE ANALYSIS; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; PRS GENE; SOX9 GENE;

CLEFT LIP; CLEFT PALATE; DATABASES, GENETIC; DNA MUTATIONAL ANALYSIS; HUMANS; MALE; PIERRE ROBIN SYNDROME;

EID: 33645016063     PISSN: 10556656     EISSN: None     Source Type: Journal    
DOI: 10.1597/05-008.1     Document Type: Article

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